Canonical Allele Identifier: CA1986002899
Gene:

Linked Data

dbSNP Id: rs1857189639
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.81143449G>A , CM000673.2:g.81143449G>A GRCh38
NC_000011.9:g.80854492G>A , CM000673.1:g.80854492G>A GRCh37
NC_000011.8:g.80532140G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_247272.2:n.46+109477C>T
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Search 100 bp 3'